Label: GLYCOLIC ACID 50 BUFFERED SKIN CHEMICAL PEEL solution
GLYCOLIC ACID 35 BUFFERED SKIN CHEMICAL PEEL solution
GLYCOLIC ACID 70 BUFFERED SKIN CHEMICAL PEEL solution

  • NDC Code(s): 84785-0016-1, 84785-0016-2, 84785-0016-3, 84785-0016-4, view more
    84785-0016-5, 84785-0017-1, 84785-0017-2, 84785-0017-3, 84785-0017-4, 84785-0017-5, 84785-0019-1, 84785-0019-2, 84785-0019-3, 84785-0019-4, 84785-0019-5
  • Packager: Gazebo Wellness SKIN LLC
  • Category: HUMAN OTC DRUG LABEL

Drug Label Information

Updated December 16, 2024

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  • DOSAGE & ADMINISTRATION

    DIRECTIONS: Apply the peel to the treatment area. Let stand on skin for 2-10 minutes depending on skin tolerance. Remove peel with copious amount of water. Follow with moisturizer. Note: A stinging sensation may occur. Flakiness may occur for 3-5 days after performing peel. When using this product avoid unnecessary sun exposure and use sunscreen. For external use only.

  • WARNINGS

    DIRECTIONS: Apply the peel to the treatment area. Let stand on skin for 2-10 minutes depending on skin tolerance. Remove peel with copious amount of water. Follow with moisturizer. Note: A stinging sensation may occur. Flakiness may occur for 3-5 days after performing peel. When using this product avoid unnecessary sun exposure and use sunscreen. For external use only.

  • INACTIVE INGREDIENT

    Inactive ingredient: Deionized Water.

  • INDICATIONS & USAGE

    Apply the peel to the treatment area. Let stand on skin for 2-10 minutes depending on skin tolerance. Remove peel with copious amount of water. Follow with moisturizer. Note: A stinging sensation may occur. Flakiness may occur for 3-5 days after performing peel. When using this product avoid unnecessary sun exposure and use sunscreen. For external use only.

  • KEEP OUT OF REACH OF CHILDREN

    keep out of reach of children

  • PURPOSE

    glycolic acid skin peel
    BUFFERED 50%
    Clears Acne & Scars Removes Dead Skin Cells Prevents Fine lines & Wrinkles

    Distributed By:
    Skin Beauty Solutions Elk Grove CA 95759

  • ACTIVE INGREDIENT

    Active ingredients: MD Grade Glycolic Acid, Sodium Lactate.

  • PRINCIPAL DISPLAY PANEL

    Content of labeling

    Content of labeling 60 mlContent of labeling 60 mlContent of labeling Content of labeling Content of labeling 60 mlContent of labeling 30 mlContent of labeling Content of labeling 30 mlContent of labeling 30 ml

  • INGREDIENTS AND APPEARANCE
    GLYCOLIC ACID 50 BUFFERED SKIN CHEMICAL PEEL 
    glycolic acid 50 buffered skin chemical peel solution
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:84785-0016
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    GLYCOLIC ACID (UNII: 0WT12SX38S) (GLYCOLIC ACID - UNII:0WT12SX38S) GLYCOLIC ACID0.3 mg  in 30 mL
    SODIUM LACTATE (UNII: TU7HW0W0QT) (LACTIC ACID - UNII:33X04XA5AT) SODIUM LACTATE0.3 mg  in 30 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:84785-0016-130 mL in 1 BOTTLE; Type 0: Not a Combination Product10/01/2024
    2NDC:84785-0016-260 mL in 1 BOTTLE; Type 0: Not a Combination Product10/01/2024
    3NDC:84785-0016-3120 mL in 1 BOTTLE; Type 0: Not a Combination Product10/01/2024
    4NDC:84785-0016-4240 mL in 1 BOTTLE; Type 0: Not a Combination Product10/01/2024
    5NDC:84785-0016-5480 mL in 1 BOTTLE; Type 0: Not a Combination Product10/01/2024
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01610/01/2024
    GLYCOLIC ACID 35 BUFFERED SKIN CHEMICAL PEEL 
    glycolic acid 35 buffered skin chemical peel solution
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:84785-0019
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    GLYCOLIC ACID (UNII: 0WT12SX38S) (GLYCOLIC ACID - UNII:0WT12SX38S) GLYCOLIC ACID0.3 mg  in 30 mL
    SODIUM LACTATE (UNII: TU7HW0W0QT) (LACTIC ACID - UNII:33X04XA5AT) SODIUM LACTATE0.3 mg  in 30 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:84785-0019-130 mL in 1 BOTTLE; Type 0: Not a Combination Product10/01/2024
    2NDC:84785-0019-260 mL in 1 BOTTLE; Type 0: Not a Combination Product10/01/2024
    3NDC:84785-0019-3120 mL in 1 BOTTLE; Type 0: Not a Combination Product10/01/2024
    4NDC:84785-0019-4240 mL in 1 BOTTLE; Type 0: Not a Combination Product10/01/2024
    5NDC:84785-0019-5480 mL in 1 BOTTLE; Type 0: Not a Combination Product10/01/2024
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01610/01/2024
    GLYCOLIC ACID 70 BUFFERED SKIN CHEMICAL PEEL 
    glycolic acid 70 buffered skin chemical peel solution
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:84785-0017
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    SODIUM LACTATE (UNII: TU7HW0W0QT) (LACTIC ACID - UNII:33X04XA5AT) SODIUM LACTATE0.3 mg  in 30 mL
    GLYCOLIC ACID (UNII: 0WT12SX38S) (GLYCOLIC ACID - UNII:0WT12SX38S) GLYCOLIC ACID0.3 mg  in 30 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:84785-0017-130 mL in 1 BOTTLE; Type 0: Not a Combination Product10/01/2024
    2NDC:84785-0017-260 mL in 1 BOTTLE; Type 0: Not a Combination Product10/01/2024
    3NDC:84785-0017-3120 mL in 1 BOTTLE; Type 0: Not a Combination Product10/01/2024
    4NDC:84785-0017-4240 mL in 1 BOTTLE; Type 0: Not a Combination Product10/01/2024
    5NDC:84785-0017-5480 mL in 1 BOTTLE; Type 0: Not a Combination Product10/01/2024
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01610/01/2024
    Labeler - Gazebo Wellness SKIN LLC (119609953)
    Registrant - Gazebo Wellness SKIN LLC (119609953)
    Establishment
    NameAddressID/FEIBusiness Operations
    Gazebo Wellness SKIN LLC119609953manufacture(84785-0019, 84785-0017, 84785-0016)
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